Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2016 2019
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179 		0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs77786029
rs77786029 		12 122496512 intron variant C/T snv 2.9E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs77786029
rs77786029 		12 122496512 intron variant C/T snv 2.9E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019